একটি monosaccharide চিনি যে এ্যাল্ডেহাইড গ্রুপ রয়েছে বা hemiacetal হয়

aldoses's Usage Examples:

Aldoses with alcohol groups on the right of the Fischer projection are D-aldoses, and those with alcohols on the left are L-aldoses.

D-aldoses are.

groups: the aldoses, which have an aldehyde group, and the ketoses, which have a ketone group.

Ketoses must first tautomerize to aldoses before they can.

monosaccharide ketoses are reducing sugars, because they can tautomerize into aldoses via an enediol intermediate, and the resulting aldehyde group can be oxidised.

principle that, when heated, ketoses are more rapidly dehydrated than aldoses.

It is the simplest of all common aldoses.

Ribulose has the same stereochemistry at carbons 3 and 4 as the five-carbon aldoses ribose and arabinose.

Aldehyde monosaccharides may be called aldoses; ketone monosaccharides may be called ketoses.

gives a positive test because the base in the reagent converts it into the aldoses glucose and mannose.

, which is further classified in to aldoses and ketoses depending on the type of functional group present in them.

found in many biological systems, and are the products of the oxidation of aldoses by Benedict's or Fehling's reagents.

degradation in carbohydrate chemistry is a chain contraction method for aldoses.

isomerases, specifically those intramolecular oxidoreductases interconverting aldoses and ketoses.

Aldaric acids are usually synthesized by the oxidation of aldoses with nitric acid.

aldoses's Meaning':

a monosaccharide sugar that contains the aldehyde group or is hemiacetal